[Genetic and clinical analysis of X-linked hypophosphatemic rickets].

Wei, L Y; Gong, C X; Cao, B Y; Li, X Q; Liang, X J; Li, W J; Wu, D; Liu, M; Su, C; Chen, J J

Wei, L Y; Gong, C X; Cao, B Y; Li, X Q; Liang, X J; Li, W J; Wu, D; Liu, M; Su, C; Chen, J J.

Afiliação

Wei LY; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Gong CX; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Cao BY; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Li XQ; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Liang XJ; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Li WJ; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Wu D; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Liu M; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Su C; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Chen JJ; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.

Zhonghua Er Ke Za Zhi ; 59(8): 678-683, 2021 Aug 02.

Article em Zh | MEDLINE | ID: mdl-34333921

Assuntos

Raquitismo Hipofosfatêmico Familiar; Doenças Genéticas Ligadas ao Cromossomo X; Criança; Pré-Escolar; Éxons; Raquitismo Hipofosfatêmico Familiar/genética; Feminino; Doenças Genéticas Ligadas ao Cromossomo X/genética; Humanos; Lactente; Masculino; Endopeptidase Neutra Reguladora de Fosfato PHEX/genética; Fenótipo; Estudos Retrospectivos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Genéticas Ligadas ao Cromossomo X / Raquitismo Hipofosfatêmico Familiar Tipo de estudo: Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: China

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